Date published: 2025-9-12

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MPZL1 Activators

MPZL1 Activators encompasses a group of chemical compounds identified to modulate the activity or expression of MPZL1, a significant component in cell signaling pathways. Trichostatin A and SAHA are notable members of this class, operating by inhibiting histone deacetylase, leading to altered gene expression and subsequently impacting MPZL1 activity. 5-Azacytidine, another member, modifies DNA methylation patterns, inducing changes in gene expression, including that of MPZL1. Further, compounds like Rapamycin and Y-27632 have distinct mechanisms, such as mTOR inhibition and modulation of cell morphology and migration via ROCK inhibition, respectively, contributing to the variety in this chemical classification and offering multiple points of interaction with MPZL1.

In addition, chemicals like PD98059 and SB203580 intervene in different cellular processes and signaling pathways like the MAPK/ERK and p38 MAPK, influencing the operational environment of MPZL1. Cyclopamine and DAPT, by modifying the Hedgehog and Notch signaling pathways respectively, join the array of compounds that affect the signaling landscape in which MPZL1 functions. LY294002 and U0126, affecting PI3K and MEK respectively, complete this diversified class by providing additional pathways through which the activity or expression of MPZL1 might be modulated.

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